Tag | Content |
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EnhancerAtlas ID | HS187-06045 |
Organism | Homo sapiens |
Tissue/cell | Th1 |
Coordinate | chr12:92771650-92774190 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nr2f6(var.2) | MA0728.1 | chr12:92773320-92773335 | TGACCTCTTGACCTC | - | 8.55 | TCF7L2 | MA0523.1 | chr12:92772810-92772824 | AGCCTTTGATCTTC | - | 6.32 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH12I092378 | chr12 | 92772523 | 92773592 |
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Enhancer Sequence | ATTCTAGACC TTGTATATCC TCAGCCTTGG CTTCAGAATG TTGGAGACAT GATGCCAATT 60 CCAGTTCACA ACAAAGCAGC ATACGTAGTA ACCCAGATTG TCTCCCGGCC ACTGAATATT 120 GACCCAATGC TGTTCATTGC TGTTGAGAGC ACTAAACTTC TCTTCAAACC AACCAGCAGC 180 TGCAGGAGTG AAAAAAGAGT GTGAGACAAT AGCGTCTGAG TTTACCAACA CTTCGATCAT 240 TCGAAGCCTT TACAGATAAA TCATCTTCAA GAGAATAAGT GCTCCCCAAG TGTATACTTA 300 TGCTGGCGGT TGAAGGGATC TTGCCTGTAG ATGCTCTGAT GCTTCAGAAA AGAGAAAGGA 360 AAGGAGGTCT GGGTCCCTTG TCCCAGCCTG TGGGGTCTCT AGAGAATTCG TCACAACCAC 420 TCTCCTACCC CCTAAAATAT GGAGGTTGGG CTGAGCCACA GGCAGGCAGG CAAATCTACT 480 GCAAGCTCCC TTACATTTTT CTATGGCGTT CCATGGGGTA AAGAAAGTTT CCCCAAGGAT 540 TTTGCTTCAC TCTAACAATG GGACAGAAAA GAATTTAGGA GGAGAGCATA AGTCCATTTA 600 AAACTGCATA TAAATGATAT ATTGTGATCA TATACATATA GTGATCAACA TCTTGCTCTC 660 CCACTTTTCA GAGCCCTTTC CCACACATGG GCTTGTGTGA AGCTGAGTAA AAGGAGCAAA 720 GGTTTTGGGG TCCGGACTCG AGTTCGGATC CTGGCTTTTC CACTCACCAT GTTGCTTACC 780 TCTCCAAGCC TCAGTTTCCA ATGTTTCCAC TAAACAGCTT TGTTGTGAAT GGAGTTAGAT 840 AATAGAGGTA ACGCCCCCAA AACATGGTAT GCACTTGAGA AATGATAGCT CTCCCATCAT 900 CCACAGCACA TCACACACAG AAGTCATTAT CCAGGTGTTT GTTGAAGAAC TAGCTTCATT 960 TTGCAGATGA GAACACTGAG ACTCTGAGAG GTCAACTGAC TTGCCCAAGG TCACAGCTAG 1020 CAAGAGGGTA GTTTTCTCAT TACAAATCTG TGCCCCAAGC AATATTCTTT TATGCAACCT 1080 TTGGGTTTGG AGTTGTACTT CTAGGTAGGT CAGATACCAG AATGAAGAAA AATATTCAGG 1140 AAGGTCTGTT CTTTGAAATC AGCCTTTGAT CTTCACCAAA ACTGCCTTGC AATTTTCAAT 1200 CATGAAACCT TTGCAAAGGG TTGTTTCCTC AGAAGCCTGT GTTCAAACCT CACACTTCTG 1260 TGAAATAACT GCTTTATGCC TTAAGACTGT CGATTTGTGT TTGAGTTCAG ACATTTGGTA 1320 AGTGGAGGAT GTTTTGAAGG TATTATCAGT CACTGTCTCA TCCATAGACT GGATGAAAGG 1380 GTCGGCATCA CAGTCACATG GCTTTGCTAA ATTGTCCTGT GTCTTATCTT TGTCTGACAG 1440 CAGCAGAGCA CACCAGATAG GAGGGCACTG TCAGAACACT CTTGAATACC TTAGCCTATG 1500 CCAAAAACAG ATGAAGATAT GGTTGAAGAA ATACGGCTCA AGTAACTAAG AATCATTGCT 1560 ACATCAACTA TTGTAGCATG AAGCTGCATT GGCTGTGTTT ATGGTCTCTT TTAGCTTAAA 1620 AATACTATGC CATTTTATTC CACTCCTCTG CTCCATACCA GTTTTATTGT TGACCTCTTG 1680 ACCTCTTAAA AGTTTGGTCA CATCTGGGGC ATCCTGCAAC AGCAGTGCTT CCTATTGAAA 1740 AAATTAAATT GAGGTGGGCC AAGACCTGGT CTGTCCAAAA TATGTAGCCC TAAGCACCCT 1800 GCTCTTTGTA AACGATGATA ATATTGCCGA CCCAGGGACA GAGTTCTTTT TTGCGTGCAA 1860 ATAAAGCTCA AAATCCAAGA GGCACTGGTA CCATTTTTTA AAGGCCTACA CCAGTAAAGA 1920 CTATCTGCTC CTCCATCTAT CCTTCTCTTT GACCTTCTAA TTTTTACTCT TCAAATATCT 1980 CTTGGTCACC TGTTATATTT CAGGCACAGT GCTAGATACA AGGACTGTGG CTGAACTCTC 2040 ATAGAGATTA TAGTAGGAAA GATAGACAAA AACAAATCAT TTCACAAAAA TTTAAGAAGA 2100 GGCATGCTTC AAGGAGAAGG ATGCCAGGAG TGGGCAGATA GGACATCCTA AGAGAGACAA 2160 TTTAGCCAAA TGCCTGAGAG AATGATGGGC TCTGGAATCT GCCCAAGAGG CTCAAGTCTT 2220 ATTCTTCCTC TCACCATCCC TGTGACAGTA GCCAGTTGCT TAATCGCTCT GTGCCTCAGT 2280 TTCCCCAGCT ATAATATGAA GCTATAATAG TACCTTCCTC TCAGGGTTGC TGTGGAGATT 2340 AACTGAGATA GCACATGTGA AGCATGTAGA ACAACATCTG GTACTAGCAA GTGTTCAGCC 2400 TGGGGTGGGG AACATACCTG ACCTGTGCTA CCTGTGGACC TCTCTAAGCA AGTAAGCTGG 2460 GACATGAAAA TAAATAAAGA TAAGCATAGC AAACCACCAT GACACATGTT TACCTGCGTA 2520 ACAAACCTTC ACATCCTGCA 2540
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